Double Beam Spectrophotometer Research Articles

Enhancement of the photodegradation performance towards methylene blue and rhodamine B using AgxSn1–xO2 nanocomposites

In the present study, the structural properties, as well as the photodegradation performance of methylene blue (MB) and rhodamine B (Rh B) using hydrothermal synthesized AgxSn1–xO2 (0 ≤ x ≤ 1) nanocomposites were studied. The study was investigated using various techniques including EDS, XRD, FE-SEM, HR-TEM, photoluminescence spectroscopy, N2 adsorption-desorption, GC-MS, and a double-beam spectrophotometer. The tetragonal SnO2 phase dominates, while the cubic Ag2O phase appears at larger x ratios (x ≥ 0.5). The crystallite and particle sizes were slightly raised for a low Ag ratio but dramatically increased for higher x ratios. Different morphologies emerge depending on the composition, such as spherical and irregular particles for x = 0 and 1, sheet-like morphology for x = 0.05, 0.2, and 0.4, and worm-like morphology for x = 0.5. The maximum surface area was calculated using the BET method to be 358 and 354 m2/g for x = 0.2 and 0.4, respectively. The direct optical band gap depends on the x ratio and the crystallite size and equals 3.95eV and 3.70eV for x = 0 and x = 1, respectively. The synthesized AgxSn1–xO2 composites demonstrated excellent photodegradation efficiency (η) towards MB and Rh B. The majority of compositions had high η towards MB and the highest value of 99.6% was attained using Ag0.4Sn0.6O2 under the UV-visible irradiation for 1.5h. Also, synthetic composites demonstrated efficient photodegradation of Rh B, particularly for higher Ag content (η = 94.4% at x = 0.5). The catalysts revealed acceptable reusability and stability, and the degraded products were studied using the GC-MS technique with a proposed mechanism of degradation. The improvement in photodegradation of MB and Rh B dyes can be attributed to an increase in surface area, as well as the development of shape and optical characteristics.

Formulation and evaluation of extended-release floating tablets of labetalol hydrochloride 200 mg

The aim of present work is to formulate and evaluate extended-release floating tablets of Labetalol HCL to improve the bioavailability, Patient compliance and solubility on oral floating drug of Labetalol HCL. Labetalol HCL is mainly used in the treatment of hypertension, which is BCS Class Ⅰ drug i.e. Highly soluble and highly permeable. The tablets were prepared by wet granulation method by using different concentrations of HPMC polymer. The tablets were evaluated for Preformulation characteristics, Pre compression parameters and post compression parameters. In-vitro dissolution studies were performed for all prepared formulations by using dissolution test apparatus employing a paddle stirrer at 50 rpm and 37 ± 0.5°C, 0.1N HCL buffer was used as dissolution medium. Samples of 5ml each were withdrawn at different time intervals. Each sample withdrawn was replaced with an equal amount of fresh dissolution medium. Samples were diluted and assayed at 302 nm using Agilent UV Visible double beam spectrophotometer. The increased drug release is due to the presence of low concentration of HPMC K4 m. The drug release kinetics was calculated for all the formulations, among all the formulations F8 was taken as optimized formulation whose percentage drug release was found to be 96%. It indicates the release follows zero order and Hixon kinetics. Hence formulation F8 was Considered as the optimized batch and stability studies were conducted at 40oc±2oc/75±5%RH, Storage condition for 3 months and no change was observed.

Influence of a plasma focus device on the structural and optical properties of highly conductive AZO thin films

In the present work, we deposited Al-doped ZnO (AZO) thin films on microscope glass slides at different pressures (5, 10, 20, and 30 mTorr) using an EAEA-PFD (Plasma Focus Device of the Egyptian Atomic Energy Authority) without any extra heat treatment. Argon gas provided the radiant energy needed to form a crystalline AZO film. This study investigated the deposition and features of AZO thin films. The impact of changes in work pressure on the microstructure, morphology, and optical attributes of AZO films was reported. The results demonstrated that varying the work pressure significantly affects the microstructure, morphology, crystallinity, optical absorbance, and optical energy gap. The microstructure and morphology were evaluated through XRD and scanning electron microscopy (SEM). The optical properties were analyzed using a UVvis double-beam spectrophotometer within a wavelength range from 300 to 1100 nm. XRD patterns indicating a zinc-blende structure and the Williamson–Hall approach were used to estimate the structural parameters. The estimated trend in the particle size of the AZO film demonstrates a decrease from 82 ± 5 nm to 48 ± 5 nm as the pressure increases. The calculated energy gap, Egopt, increases from 3.53 eV to 3.69 eV with increasing work pressure. The conductivities in terms of both optical and electrical decreased with increasing work pressure of the AZO films.

Effect of Li Doping on Structural, Optical, and Optoelectrical Characteristics of ZnSnO3 Thin Films Prepared by Nebulizer Spray Pyrolysis

In this work, ZnSnO3 (ZTO3) and Li-doped ZTO3 thin films were synthesized on glass slides by a cost-effective nebulizer spray pyrolysis procedure. The X-ray diffraction analysis revealed that the ZTO3 and Li-doped ZTO3 thin films possessed a rhombohedral structure. The structural indices (grain size, dislocation density, lattice strain) of the ZTO3 and Li-doped ZTO3 thin films were computed. The morphology characteristics of the ZTO3 and Li-doped ZTO3 thin films were observed by field emission scanning electron microscopy. The inspected films display uniform and homogeneous surfaces. The optical transmittance, T, and reflectance, R, of the ZTO3 and Li-doped ZTO3 thin films were recorded using a double-beam spectrophotometer to investigate the optical characteristics of these layers. The refractive index of the ZTO3 and Li-doped ZTO3 thin films was enhanced via the Li content increase. Moreover, Tauc’s plots demonstrated that the energy gap of the ZTO3 and Li-doped ZTO3 thin films was reduced from 3.85 eV to 3.08 eV by boosting the Li doping content. Moreover, the increase in Li content produces an enhancement in the optoelectrical indices (optical resistivity, optical carrier concentration, optical mobility, plasms frequency, and optical conductivity) of the ZTO3 and Li-doped ZTO3 thin films. The nonlinear optical indices of the ZTO3 and Li-doped ZTO3 thin films were deduced, and it was noted that Li content boosted the nonlinear optical indices of these layers. All the ZTO3 and Li-doped ZTO3 thin films displayed n-type semiconducting properties by the hot probe equipment.

Effect of air-abrasion pretreatment with three desensitizing agents on efficacy of in-office tooth bleaching.

To evaluate the influence of air-abrasion of enamel with three different desensitizing powders on the whitening effect of a bleaching gel containing 40% H2O2, which was used for in-office tooth bleaching. Forty human incisors, extracted and prepared, were acquired for this study and subsequently randomized into four groups (n = 10). The control group specimens underwent no pretreatment prior to the bleaching procedure, whereas the remaining three groups underwent air abrasion using distinct desensitizing powders; (a) Sylc, which contains bioglass 45S5; (b) BioMinF, which contains calcium phospho-fluoro-silicate glass; and (c) MI Pearls, which contains nano-hydroxyapatite, 1 h preceding the Opalescence Boost PF 40% bleaching procedure. Color measurements were conducted using a double-beam UV-Vis spectrophotometer at four distinct time points (prior to bleaching, 24 h, 15 days, and 30 days post-bleaching). Tooth color change outcomes revealed that there were no statistically significant results with respect to the interaction of the two criteria (treatments and time) (p = 0.990). Additionally, there were no statistically significant results with respect to the main effects of treatments (p = 0.385), while there were statistically significant effects with respect to the time criterion (p = 0.013). The use of the tested desensitizing powders prior the bleaching procedure did not affect the tooth color change induced by the tested bleaching agent. Tooth color change and whiteness are not affected by air-abrasion desensitizing treatments when applied prior to in-office bleaching procedures.

Dual solution synthesis of Al doped CuS thin films for optoelectronic and photovoltaic applications

Dual Solution Synthesis (DSS) was used to deposit CuS doped with Al. The Samples were subjected to annealing under varying temperatures of 319K and 373K . The thin films were firmly adherent to the substrates. The optical properties were measured using UV -1800 series double beam spectrophotometer. The transmittance is from 0.3% to 0.6% while the reflectance is between 0.176 to 0.204, as the wavelength ranges from 320nm to 1000nm; the average band gap obtained is 2.6. The thicknesses achieved are 100nm and 124 nm. Other Optical properties were determined for each sample which makes it suitable for applications in optoelectronic, solar energy conversions, solar cells, thin film absorbers, anti- reflective coating, aesthetic windows, UV filter and other uses.

QbD Assisted Development and Validation of UV Spectroscopic Method in Estimation of Silymarin

Background: Silymarin is a flavonoid utilised in liver dysfunction for years; new studies have emphasised its potential utility as a therapy for nanoparticulate targeting in many other disorders. In order to establish the product quality of such compounds, researchers have been trying to develop a robust method of analysis, but the methods developed till now are too expensive and time-consuming. Here we proposed quality by design-assisted development and validation of the UV spectroscopic method using Design-Expert® software in the estimation of Silymarin for fabrication of nanoparticulate formulations, which is simple, accurate, cost-effective and non-tedious. Aim: The proposed method is a simple, new, robust, accurate, and precise UV visible spectroscopic technique for estimating silymarin produced in nano-formulations utilising an analytical quality by design (AQbD) approach. Methods: A UV spectrophotometric technique was established, as maximum absorption (287.7) was measured using a Shimadzu UV-1800 double-beam UV visible spectrophotometer. The characterization of silymarin was done by melting point, DSC and FTIR techniques. The two critical method variables chosen were scanning speed and sample interval to be analysed by the design of experiment methodology utilizing the central composite design principle, which shows robustness and optimized technique involved in this work. Results: The spectroscopy technique was developed and validated as per International Conference of Harmonization recommendations. The Beer's-Lambert rule was followed in a series of 2-12 μg/ml dilution increments, with a correlation value of R2 = 0.999. The method's linearity was shown to be excellent across the concentration range. The percent recovery of the current method approach was determined to be within the confidential limitations, i.e., less than 2% expressed as % RSD, and the methodology was proved to be precise at inter and intraday variations (% RSD). The LOD and LOQ were found to be 0.264 μg/ml and 0.801 μg/ml which were also determined correctly. During specificity testing, no interfering peaks were found. Conclusion: This UV approach has been used successfully to determine the quantity of silymarin present in the nanoparticulate formulation, which can be used for testing its other pharmaceutical dosage forms.

Exploring Serum Zinc and Copper Levels as Potential Biomarkers in Polycystic Ovary Syndrome: A Cross-Sectional Study From Northeast India.

Introduction Polycystic ovary syndrome (PCOS) is a prevalent hormonal disorder characterized by irregular menstrual cycles, ovarian cysts, and elevated androgen levels. The potential association between trace elements, specifically copper (Cu) and zinc (Zn), and PCOS has been explored, but a definitive relationship remains unclear. This study aims to investigate the levels of these trace elements in women with PCOS and their potential implications. Methods The study, conducted at Gauhati Medical College & Hospital, involved 60 individuals with PCOS and a matched control group. Ethical approval was obtained, and participants provided written informed consent. The study spanned from July2021to June2022, utilizing a hospital-based case-control study design. Diagnostic criteria adhered to the Rotterdam criteria, and serum copper and zinc levels were quantified using a double-beam UV spectrophotometer. Results In the PCOS group, the mean age was 23.01 ± 3.60 years, while the control group had a mean age of 23.34 ± 3.59 years, with no significant age difference. Mean copper levels were 147.32 ± 16.53 μg/dl in PCOS and 106.88 ± 15.60 μg/dl in controls, indicating a significant increase in PCOS (p < 0.0001). Mean zinc levels were 93.99 ± 6.76 μg/dl in PCOS and 85.42 ± 12.69 μg/dl in controls, also significantly higher in PCOS (p < 0.0001). Conclusion The study highlights significant differences in serum copper and zinc levels between women with PCOS and healthy controls, suggesting potential implications for the syndrome's pathophysiology. Further research is warranted to elucidate the precise roles of these trace elements in PCOS and explore therapeutic interventions.

Antioxidant Activities and Phenolic Composition of Sarcococca saligna Leaves

Abstract: Sarcococca saligna (D. DON) Muel is a vital plant with several steroidal alkaloids and is effective against syphilis, liver diseases, gastrointestinal tract disease, infections, and inflammation. The present study aimed to investigate the in vitro antioxidant activities and phenolic profile of S. saligna. High-performance liquid chromatography (HPLC) analysis has shown the presence of twelve phenolics namely kaempferol-3-O-glucoside, proanthocyanidin B1, quercetin-3-malonylglucoside- 7-glucoside, kaempferol-3-O-sophorotioside, Isorhamnetin-3-O-glucoside-7-Orhamnoside, kaempferolhexoside, 4-O-Caffeoyl-5-O-p-coumaroylquinic acid, 3,4-Di-O-caffeoyl-5- O-feruloylquinic acid, 3,4-Di-O-feruloyl-5-O-caffeoylquinic acid, flavogalloyl-HHDP-gluconic acid (lagerstannin B), 3,4-di-O-caffeoylquinic acid and kaempferol-3-(caffeoyldiglucoside)-7-glucoside. The hot water extract showed the highest anti-lipid peroxidative activities. The IC50 value for 2,2- diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity was 71.5 ± 2.1 μg/mL. The extract could chelate the iron and possess reducing activities on phosphomolybenum assay. It is concluded that extracts of S. saligna are rich in antioxidants and contain essential phytochemicals. objective: The present study was aimed to investigate thein vitro antioxidant activities and phenolic profile of S. saligna. HPLC analysis has shown the presence of twelve phenolics namely kaempferol-3-O-glucoside, proanthocyanidin B1, quercetin-3-malonyl-glucoside-7-glucoside, kaempferol-3-O-sophorotioside,Isorhamnetin-3-O glucoside-7-O-rhamnoside,kaempferolhexoside, 4-O-Caffeoyl-5-O-p-coumaroylquinic acid, 3,4-Di-O-caffeoyl-5-O-feruloylquinic acid, 3,4-Di-O-feruloyl-5-O-caffeoylquinic acid, flavogalloyl-HHDP-gluconic acid (lagerstannin B), 3,4-di-O-caffeoylquinic acid and kaempferol-3-(caffeoyldiglucoside)-7-glucoside. method: The chemical used were 1,10-phenathroline, Thibarbituric acid, TRIS-HCl, amominium molybdate, Iron, sodium nitroprusside. HPLC standards were purchased from Sigma-Aldrich. All the reagents were of analytical grade. Double beam spectrophotometer was used for UV-VIS spectrophotometery. The HPLC system used was Agilent 1260 Infinity HPLC system which consists of quaternary pump, degasser, auto-sampler and diode array detector (DAD). conclusion: The results have shown that S. saligna antioxidant rich extract can be effectively utilized in food and pharmaceutical industries with additional income. However, more detailed understanding of utilization of extract against degenerative diseases is required. There is also need to find out the safety and bioavailability of the plant extract for its use as nutraceutical and as a plant products.

Development of the spectrophotometric method for the determination of meldonium in capsules by using alizarine

The aim of the work was to develop a simple, rapid, economic spectrophotometric method for the determination of meldonium in capsules based on the reaction with alizarin.&#x0D; Materials and methods. Analytical equipment: double-beam UV-visible spectrophotometer Shimadzu UV 1800 (Japan), a pair of 1 cm matched quartz cells, software UV-Probe 2.62, laboratory electronic balance RAD WAG AS 200/C, pH-meter И-160МИ. Pharmacopoeial standard sample (CRS) of meldonium dihydrate (Sigma-Aldrich, (≥ 98 %, HPLC)), alizarin (Synbias), capsules Metamax (Darnytsia) 250 mg, Vasopro (Farmak) 500 mg, Mildronate (Grindex) 500 mg, dimethylformamide (“Honeywell Riedel-de Haen”).&#x0D; Results and discussion. A spectrophotometric method for determining meldonium in capsules by reaction with alizarine has been developed. The absorption maximum of the formed complex in dimethylformamide was at a wavelength of 517 nm. Stoichiometric ratios of reactive components «meldonium- alizarin» were 1:1. Validation of the developed analytical method for the determination of meldonium in medicines was carried out in accordance with the requirements of the SPhU. The optimal conditions for performing the quantitative determination of meldonium have been established: concentration of alizarin solution – 0.8 %, volume 0.8 % alizarin solution – 0.5 ml, heating time – 20 min, temperature – 95+/- 2 °C. Linearity has been in the concentration range of 0.0402- 0.1073 mg/mL, the limit of detection - 2.84 μg/mL, and the limit of quantification – 8.59 μg/mL. The eco-friendliness of the developed analytical method was carried out using the analytical eco-scale, AGREE, and GAPI methods.&#x0D; Conclusions. The developed method can be used as an arbitration method for the routine analysis of meldonium capsules

UV spectrophotometric determination of chlorthalidone in tablet dosage form by using single point standardization method

The current research endeavors to elucidate the creation of an uncomplicated, highly sensitive, swift, precise, and cost-effective UV-accepted spectrophotometric method for the quantitative assessment of Chlorthalidone. This is achieved through the utilization of a visible spectrophotometric approach employing single-point standardization and calibration plot methods, for pharmaceutical dosage forms. The equipment employed includes a double-beam UV-visible spectrophotometer, specifically the Shimadzu Model UV1800, with 1cm quartz cells and 0.2 M Sodium hydroxide serving as the solvent. Notably, an absorption maximum is identified at 219 nm. The developed method strictly adheres to Beer’s law. In the case of single-point standardization, the percentage of Chlorthalidone detected falls below the labeled claimed limit. Simultaneously, the tablet formulation is subjected to a percentage purity test using the calibration plot method, revealing that the observed quantity of Chlorthalidone is below the labeled content. This suggests a potential discrepancy in the marketed product of Chlorthalidone, indicating a probable deficiency in the therapeutic effect of the formulation due to the lower amount of Chlorthalidone present. The overall efficacy of the product hinges on the quality assurance of its constituents.

A Comparative Study of Spectrophotometric Determination of Malathion With Ammonium Meta Vanadate and Potassium Bromate

Malathion is one of the commonly used pesticides in India which is toxic as per the World Health Organization. Its residue has been found in industrial effluent, water streams, and agricultural products. Various analytical methods such as gas chromatography, infrared spectroscopy, and thin‐layer chromatography were used for identifying the concentration of pesticides in aqueous phase. Though gas chromatography is one of the best available techniques in pesticide analysis, it involves higher cost. In this study, simple spectrophotometric methods for identifying the malathion in aqueous phase are experimented and compared using UV visible double beam spectrophotometer. Comparing these two methods will help us to select the most suitable method for specific analytical needs, considering factors such as accuracy, sensitivity, ease of use, and safety. This comparative analysis aids in choosing the best method for reliable and efficient determination of malathion. A regression analysis of Beers–Lambert plots showed a good correlation in the concentration range of 0.5–15 mg/L for the abovementioned two spectrophotometrical methods. The results showed that potassium bromate exhibits rapid, stable color complex and linearity in absorbance versus concentration study when compared with ammonium meta vanadate.

Novel Time-Saving Technique to Measure the 2D Complex Profile of Spectral Transmittance of Linearly Variable Filters and Assessing Homogeneity of Optically Transparent Materials

Emerging technologies for coating new types of filters, such as linearly variable bandpass filters, urges new kind of measurement systems requiring accurate and time-saving spatially resolved transmittance measurements. On the other hand, one of the main uses of coated filters is standardization use; e.g., as certified reference materials (CRMs) for transmittance and absorbance standards. In this case, the homogeneity assessment is of great interest. To do such measurements with low uncertainty, spatial scanning methods using reference double-beam spectrophotometers are routinely used. High time consumption and relatively high-cost are disadvantages of this traditional method. In this work, we propose a new system based on an imaging technique. The newly developed system comprises a quartz tungsten halogen (QTH)-based illuminator, with collimator and coupling optics, a double-grating monochromator, customized integrating sphere, and scientific highly digitized, high-resolution and dynamic range Si-based CCD (monochrome) camera. The system is time-saving: in one-shot we may measure the spatial transmittance distribution of the samples (e.g. filters) without separately measuring the reference (air), which has many instability issues. Validation measurements using standard filters are presented. Systematic errors may be studied and corrected for. Many types of filters and liquids, for instance chemical reference materials (RMs), may be measured and reported. Uncertainty of spatial, spectral and radiometric components are studied carefully and estimated. The combined uncertainty evaluation has shown that relatively low uncertainty levels may be achieved, specially in the visible range (U &lt; 1 %, k=2 ). Spatially-resolved data with different curves at different positions (spatial points) are shown in the spectral range of 380 nm through 950 nm. The combined uncertainties at some spectral points are presented and proved to be sample- and wavelength-dependent at all the points in the field-of-view (FOV) of the CCD camera.

DEVELOPMENT AND VALIDATION OF NOVEL UV-VISIBLE SPECTROPHOTOMETRIC METHOD FOR ESTIMATION OF TEPOTINIB IN BULK AND IN PHARMACEUTICAL FORMULATION

Objective: The objective of the study is to develop a new, simple, rapid, accurate, and economical UV-spectrophotometric method and validate the same for the estimation of Tepotinib in bulk and in pharmaceutical formulation as per ICH guidelines. Methods: The present work was carried out using the UV-Visible double-beam spectrophotometer model Systronics 2201. Tepotinib was found soluble in water, methanol, methanol so, analytical-grade methanol was used as a solvent for conducting the work. The λmax of the tepotinib was determined by dissolving pure drug in methanol scanned in the range of 200-800 nm. The present method was validated for the linearity, accuracy, precision, Limit of Detection and Limit of Quantification. Results: The maximum absorbance of tepotinib obtained at a wavelength of 272 nm. The method was found linear in the range of 3-15 µg/ml with the regression coefficient of 0.996 and the equation y = 0.0699x+0.0335. The accuracy was found to be in the range of 96.8-98.5%, the intra-day and inter-day precision % RSD value was 0.262 and 0.69, respectively and the LOD and LOQ were 0.0925 µg/ml and 0.28 µg/ml respectively. Conclusion: The method demonstrated good reproducibility and recovery so, proposed method can be successfully applied for the routine analysis of tepotinib in bulk and pharmaceutical dosage form.

Antimicrobial, antioxidant, and sun protection potential of the isolated compounds from Spermacoce princeae (K. Schum)

BackgroundSpermacoce princeae (K. Schum) has been used in the treatment of bacterial skin infections in Uganda. Pharmacological studies revealed that extracts of S. princeae exhibited antibacterial, antioxidant, and sun protection potential. This study aimed at isolating and identifying pure compounds from the extracts based on comprehensive analytical characterization by multiple analytical techniques.MethodsThe plant samples were extracted by sequential maceration using n-hexane, ethyl acetate, methanol, and distilled water. The compounds were isolated using a combination of chromatographic techniques and their structures were elucidated by multiple spectroscopic techniques. The antibacterial and antifungal activity determination of the isolated compounds was carried out using an agar well diffusion and potato dextrose assay against Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, Candida albicans, and Aspergillus flavus while the antioxidant activity was screened with the 2,2-diphenyl-2-picryl-hydrazyl (DPPH) radical scavenging assay. The sun protection factor was determined using a Shimadzu Ultra Violet-visible (UV–VIS) double beam spectrophotometer between 290 to 320 nm.ResultsEleven compounds; quercetin (1), kaempferol-3-O-rutinoside (2), rutin (3, 12), myo-inositol (4), asperulosidic acid (5), hexadecanoic acid (6), β-sitosterol (7), stigmasterol (8), campesterol (9), ursolic acid (10), and β-sitosterol glucoside (11) were identified in the S. princeae extracts. Compound 2 had good antifungal activity against C. albicans (zone of inhibition, 23.0 ± 0.1 mm). Compound 10 showed antibacterial and antifungal activity against S. aureus, P. aeruginosa, C. albicans, and A. flavus. Compound 2 had a good percentage radical scavenging effect (IC50 = 64.81 µg/ml) and a good sun protection factor (SPF = 26.83).ConclusionThis study reports the first-time isolation and identification of compounds 1 to 11 from S. princeae, which contribute to its antimicrobial, antioxidant, and sun protection potential.

Heavy Metals Accumulation in Water and Human Health Risk Assessment via the Consumption of Labeobarbus intermedius Samples from Borkena River, Ethiopia

Concentrations of heavy metals, namely, chromium, lead, cadmium, and copper, were evaluated in the water samples and selected fish organs (Labeobarbus intermedius) from the Borkena River, Ethiopia. The concentrations of these metals were determined using ELICO’s SL-176 double-beam atomic absorption spectrophotometer (AAS). The distribution of heavy metals in water samples analyzed was in the order of magnitude of Cu &gt; Cr &gt; Cd &gt; Pb. The average heavy metal concentrations recorded in the water samples were below the maximum permissible limit established by international and national organizations (WHO, EPA, and USEPA), except for cadmium. Organ specificity was observed for accumulating the selected heavy metals in the order of liver &gt; kidney &gt; muscles. Pearson’s correlation results revealed that Cr and Cd originated from similar sources. Hazard quotient (HQ) and total hazard index (THI) results showed that Cu, Cr, Cd, and Pb contents were safe and might not have adverse public health effects. From the point of carcinogenic risk, this study suggests that the observed Cr and Cd concentrations possibly pose a risk of developing cancer in the future. Controlling waste at the source and implementing remediation strategies should be done to reduce heavy metal pollution in the river.

Transition metal salphen DNA complexes as biosensor application for detecting various mosquito viruses

PurposePiperidine side chain-functionalized N, N′-bissalicylidene phenylene di amine di-anion (salphen) consisting of salphen-Zn and salphen-Cu are able to intercalate with nucleic base stacking of DNA and can be applied as an optical DNA hybridization detector. Attaching DNA and salphen to glass surfaces has been done via coating the surface with the silane coupling agents containing 3-aminopropyltriethoxysilane that was synthesized for acting as a high-affinity RNA carrier matrix. The Schiff base salphen-zinc (II) and salphen-Cu (II) complexes-labelled probe to target nucleic acid renders a colour change of the DNA biosensor to a green and red background colour for zinc and copper, respectively. This study aims to indicate that the DNA biosensor data with high efficiency is used for detection of dengue virus serotypes 2 (DENV-2) and Chikungunya virus (CHIKV) concentration via salphen-Zn (II) and salphen-Cu (II), respectively, in human samples.Design/methodology/approach1H-NMR and 13C-NMR have been used via PerkinElmer LAMBDA 35 instrument. The authors also used a double beam spectrophotometer with (CH3)4Si (TMS) as reference and dimethyl sulfoxide as solvent reference in pH = 7.0. Various DNA concentrations have been used for UV spectrophotometry at 300 nm and 400 nm for zinc and copper complexes, respectively. BRUKER mass spectra with DIONEX Ultimate 3000 LC model were used for all measurements. Mettler Teledo model (DSC882e) of differential scanning calorimeter (DSC) was used for measure the melting temperature of metal zinc and copper complexes. The morphology of the silica Nano spheres (SiNs) were scanned by FESEM with Model JSM-6700F from Japan.FindingsThe Cu (II) and Zn (II)-salphen-viruses DNA system for CHIKV and DENV-2, respectively, in different concentration have been investigated via various spectroscopies (Figure 3). CHIKV and DENV-2 DNA were selected from human saliva and urine samples as models for conformations of human G4-DNA. By increasing the amounts of DNAs, and G4, the UV–Vis bands of located above 300 nm, experienced a hypochromic effect. The Cu2+ complex exhibits selectivity towards the G4, and there is a similar affinity for Zn2+ complex binds to the G4. These results collectively suggest that the Cu2+ complex is stronger than the Zn2+ complex. The authors have found copper (II) and zinc (II) compounds and nucleic acid-complexes are strongly fluorescent molecules in the low energy range, from the visible to the near-infrared. Since the fluorescent emission of Zn (II) and Cu (II) complexes are enhanced by the binding to nucleic acids upon visible light exposure when bound to DNA. These complexes are important as selective fluorescent probes for nucleic acids and to highlight their potential application. UV–vis spectroscopy is an accurate for finding the extent of ligand interaction with DNA and metallic complexes–DNA binding. Generally, the binding of intercalative compounds to DNA can be characterized through absorption spectral titrations, where lowering in absorbance (hypochromism) and shift to longer wavelengths (red shift) were observed in this work.Originality/valueThe serum samples have been provided as citrate and collected in tubes after blood is allowed to clot. Then, it has been separated by centrifugation, and the authors have kept serum refrigerated at 4°C or frozen at –20°C. It is notable; specimens have been confirmed by Centres for Disease Control (CDC)-Dengue Branch previously. For the work, these samples have been frozen previously, and the diagnostic practiced tests at the CDC-Dengue Branch have been validated in serum and plasma. Therefore, plasma separated in lavender or heparins are suitable and acceptable for serology testing.

Enhancement in microstructural and optical properties of thermally evaporated CdTe/CdSe heterojunction thin Films

The optimization of microstructural and optical properties of a thin layer is an important step prior device fabrication process, so an enhancement in these properties of thermally evaporated CdTe/CdSe thin films was reported in this work. We choose to research (CdSe) materials as a n-type absorber layer in the CdTe/CdSe heterojunction thin film. The Effect of annealing temperature on the structural and optical properties of CdTe/CdSe Heterojunction thin films was studied, using various techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM) and Double-beam computer-controlled spectrophotometer in the wavelength between 200 nm and 2500 nm. Diffraction (XRD) patterns showed that the as-prepared films were amorphous nature, whereas the annealed films were polycrystalline. These results were confirmed by scanning electron microscopy investigations. It was found that the crystallite size and degree of crystallinity of the studied films depend on the annealing temperature. Furthermore the optical measurement shows that this treatment shifts the optical absorption edge at low energy and decreases the optical band gap from 1.92 eV, to 1.37eV while the values Urbach energy increase as the annealing temperature increased from 300 K to 433 K. As consequence is that the heat treatment improves the quality of the CdTe/CdSe heterojunction thin films for the potential use in photovoltaic applications.

Development of aptamer based colorimetric assay for whole blood glycated hemoglobin (HbA1c) estimation using gold nanoparticles

Thiol-modified aptamer oligonucleotides containing gold nanoparticles (G@NPs) bound to glycated hemoglobin (HbA1c) with high affinity in whole blood samples. Aptamer thiol groups enhanced the stability of aptamers adsorbed on the surface of G@NPs. A detection strategy was used to visually confirm the presence of HbA1c and the absorbance of the colored compounds at selected wavelengths. Modified G@NPs are used in many colorimetric detection strategies due to their high extinction coefficient and strongly distance-dependent optical properties. In the present study, as the target analyte reports a method to prepare gold nanoparticle-bound purple aptamer aggregates that rapidly collapse into bluish red dispersed nanoparticles upon binding of HbA1c. HbA1c was detected in unpretreated whole blood after dilution at pH 7.4 and with UV-VIS double beam spectrophotometer with a lower limit of detection (LOD) (0.1 μM) and a much broader linear detection range (0.1 μM–100 μM). This current colorimetric method provides a rapid (7 min), accurate and high determination of whole blood HbA1c with minimal interference from uric acid, bovine serum albumin, hemoglobin, and glucose. The lower detection limit and broader linearity of aptamer-bound G@NPs hybrids improve the accuracy and precision of HbA1c measurements.

Fabrication and study of characteristics of HgSr2 Can-1CunOδ+10, (n = 1, 2 and 3) thin films superconducting

Recently, particular attention has been given to the material of Superconducting films because of its exceptional electrical and optical properties. In this work, HgSr2 Can1CunOδ+10, (n = 1, 2 and 3 ) .Thin Films Superconducting have been prepared by twostep process bulk and thin film. The optical properties were calculated absorption, transmission, reflection, band gap, coefficient of absorption, excitation coefficient and index of refraction in the range of wavelengths (300-1100) nm using a double beam spectrophotometer (UV/VIS). Structural, morphological, and electrical properties were investigated using X-ray diffraction (XRD) and AFM, Using the 4-probe technique measuring the resistivity as a function of temperature. The composite HgSr2 Ca2Cu3Oδ+10 showed an improvement in all properties the structural, electrical and optical as a result of increasing of Cu-O layers.